JP2006097020A5 - - Google Patents
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- Publication number
- JP2006097020A5 JP2006097020A5 JP2005262352A JP2005262352A JP2006097020A5 JP 2006097020 A5 JP2006097020 A5 JP 2006097020A5 JP 2005262352 A JP2005262352 A JP 2005262352A JP 2005262352 A JP2005262352 A JP 2005262352A JP 2006097020 A5 JP2006097020 A5 JP 2006097020A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- ethylhexanoate
- pivalate
- compound
- optionally
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims description 38
- 230000005855 radiation Effects 0.000 claims description 25
- 239000011230 binding agent Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 12
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 12
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical group O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims description 10
- SFRSJNAYBXEQKM-UHFFFAOYSA-M 2,2-dimethylpropanoate;2-methoxyethyl(trimethyl)azanium Chemical compound CC(C)(C)C([O-])=O.COCC[N+](C)(C)C SFRSJNAYBXEQKM-UHFFFAOYSA-M 0.000 claims description 10
- WMDLGLNAIPCRPO-UHFFFAOYSA-M 2,2-dimethylpropanoate;tetrabutylazanium Chemical compound CC(C)(C)C([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC WMDLGLNAIPCRPO-UHFFFAOYSA-M 0.000 claims description 10
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims description 10
- XUZNXNABRSCKOA-UHFFFAOYSA-M 2-ethylhexanoate;2-hydroxyethyl(trimethyl)azanium Chemical compound C[N+](C)(C)CCO.CCCCC(CC)C([O-])=O XUZNXNABRSCKOA-UHFFFAOYSA-M 0.000 claims description 10
- KQSZRCPDBKWQGB-UHFFFAOYSA-M 2-ethylhexanoate;tetrabutylazanium Chemical compound CCCCC(CC)C([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC KQSZRCPDBKWQGB-UHFFFAOYSA-M 0.000 claims description 10
- DVSPHWCZXKPJEQ-UHFFFAOYSA-N 2-methoxyethyl(trimethyl)azanium Chemical compound COCC[N+](C)(C)C DVSPHWCZXKPJEQ-UHFFFAOYSA-N 0.000 claims description 10
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 claims description 10
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims description 10
- 229960001231 choline Drugs 0.000 claims description 10
- 229950010765 pivalate Drugs 0.000 claims description 10
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- -1 alicyclic carboxylic acid Chemical class 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000003863 ammonium salts Chemical class 0.000 claims description 5
- 150000004714 phosphonium salts Chemical class 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 2
- 239000008199 coating composition Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 239000003999 initiator Substances 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- 238000007142 ring opening reaction Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 4
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004043539.1 | 2004-09-09 | ||
| DE200410043539 DE102004043539A1 (de) | 2004-09-09 | 2004-09-09 | Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006097020A JP2006097020A (ja) | 2006-04-13 |
| JP2006097020A5 true JP2006097020A5 (enExample) | 2008-10-23 |
| JP4841906B2 JP4841906B2 (ja) | 2011-12-21 |
Family
ID=35462558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005262352A Expired - Fee Related JP4841906B2 (ja) | 2004-09-09 | 2005-09-09 | 化学線硬化性の基を含有する低粘度アロファネート |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9085656B2 (enExample) |
| EP (1) | EP1634902B1 (enExample) |
| JP (1) | JP4841906B2 (enExample) |
| CN (1) | CN1746244B (enExample) |
| CA (1) | CA2518137C (enExample) |
| DE (1) | DE102004043539A1 (enExample) |
| ES (1) | ES2614460T3 (enExample) |
| MX (1) | MXPA05009605A (enExample) |
| TW (1) | TWI391415B (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004043538A1 (de) * | 2004-09-09 | 2006-03-16 | Bayer Materialscience Ag | Herstellung von neuen strahlenhärtenden Bindemitteln |
| DE102004043540A1 (de) * | 2004-09-09 | 2006-03-30 | Bayer Materialscience Ag | Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen |
| DE102004043537A1 (de) * | 2004-09-09 | 2006-03-16 | Bayer Materialscience Ag | Herstellung von neuen strahlenhärtenden Bindemitteln |
| DE102005048823A1 (de) * | 2005-10-10 | 2007-04-12 | Bayer Materialscience Ag | Reaktivsysteme, deren Herstellung und Verwendung |
| US20070129568A1 (en) * | 2005-12-06 | 2007-06-07 | Ngimat, Co. | Ionic liquids |
| DE102007040239A1 (de) * | 2007-08-25 | 2009-05-07 | Bayer Materialscience Ag | Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen |
| DE102007040240A1 (de) * | 2007-08-25 | 2009-02-26 | Bayer Materialscience Ag | Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen |
| WO2010136105A2 (en) * | 2009-05-28 | 2010-12-02 | Merck Patent Gmbh | Ammoniumcarboxylates |
| RU2013138465A (ru) | 2011-01-20 | 2015-02-27 | Аллнекс АйПи С.а.р.л., | Неводные полиуретановые покрывающие композиции |
| US20140275320A1 (en) | 2013-03-14 | 2014-09-18 | Allnex IP S.à.r.I. | Methods for making elastomers, elastomer compositions and related elastomers |
| FR3003255B1 (fr) * | 2013-03-14 | 2015-10-02 | Vencorex France | Allophanate polyacrylate |
| FR3011840B1 (fr) * | 2013-10-14 | 2016-10-28 | Arkema France | Urethanes acrylates pour revetements reticulables |
| WO2020131185A2 (en) | 2018-09-26 | 2020-06-25 | Dvorchak Enterprises Llc | One component uv curable compositions and methods for making same |
| CN115677965B (zh) * | 2022-09-15 | 2023-07-04 | 南京贝迪新材料科技股份有限公司 | 一种高性能量子点复合物的制备方法 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB994890A (en) | 1961-12-18 | 1965-06-10 | Ici Ltd | New organic polyisocyanates and their manufacture |
| DE2312391A1 (de) | 1973-03-13 | 1974-09-19 | Bayer Ag | Pulverfoermige, vernetzbare ueberzugsmittel |
| DE2729990A1 (de) * | 1977-07-02 | 1979-01-18 | Bayer Ag | Verfahren zur herstellung von isocyanatgruppen aufweisenden allophanaten |
| JPS5974112A (ja) | 1982-10-20 | 1984-04-26 | Matsushita Electric Works Ltd | ラジカル重合性プレポリマ−の製法 |
| US4503226A (en) * | 1984-04-30 | 1985-03-05 | Olin Corporation | Process for trimerizing organic polyisocyanates |
| DE4416321A1 (de) | 1994-05-09 | 1995-11-16 | Bayer Ag | Verfahren zur Herstellung von Allophanatgruppen aufweisenden lichtechten Polyisocyanaten |
| US5461135A (en) | 1994-09-23 | 1995-10-24 | Olin Corporation | Polyisocyanates containing uretidione and allophanate groups, a process for their production, and their use in one and two component coating compositions |
| US5854360A (en) * | 1994-10-21 | 1998-12-29 | Sanyo Chemical Industries Ltd. | Curable composition |
| DE4441176A1 (de) * | 1994-11-18 | 1996-05-23 | Bayer Ag | Allophanatgruppen aufweisende Polyisocyanate |
| CA2189836C (en) * | 1995-12-04 | 2004-05-25 | Angela S. Rosenberry | Coating composition and floor covering including the composition |
| DE19632951A1 (de) | 1996-08-19 | 1998-02-26 | Bayer Ag | Verfahren zur Herstellung von aliphatischen und/oder cycloaliphatischen und/oder Isocyanatgruppen aufweisenden Allophanaten |
| US5739251A (en) * | 1997-03-27 | 1998-04-14 | Bayer Corporation | Low viscosity, ethylenically unsaturated polyurethanes containing allophanate groups |
| US5777024A (en) | 1997-04-30 | 1998-07-07 | The Valspar Corporation | Urethane resins and coating compositions and methods for their use |
| DE19860041A1 (de) * | 1998-12-23 | 2000-06-29 | Basf Ag | Durch Addition an Isocyanatgruppen als auch durch strahlungsinduzierte Addition an aktivierte C-C-Doppelbindungen härtbare Beschichtungsmittel |
| JP4678466B2 (ja) | 2001-08-09 | 2011-04-27 | Ｄｉｃ株式会社 | エネルギー線硬化型樹脂組成物 |
| DE10205608A1 (de) | 2002-02-11 | 2003-08-21 | Degussa | Bei niedriger Temperatur härtbare feste uretdiongruppenhaltige Polyurethan-Pulverlackzusammensetzungen |
| DE10320266A1 (de) * | 2003-05-03 | 2004-11-18 | Degussa Ag | Feste Uretdiongruppenhaltige Polyurethan-Pulverlackzusammensetzungen bei niedriger Temperatur härtbar |
| DE10346957A1 (de) * | 2003-10-09 | 2005-05-04 | Degussa | Hochreaktive, flüssige uretdiongruppenhaltige Polyurenthansysteme, die bei niedriger Temperatur härtbar sind |
| DE102004043537A1 (de) * | 2004-09-09 | 2006-03-16 | Bayer Materialscience Ag | Herstellung von neuen strahlenhärtenden Bindemitteln |
| DE102004043538A1 (de) | 2004-09-09 | 2006-03-16 | Bayer Materialscience Ag | Herstellung von neuen strahlenhärtenden Bindemitteln |
| DE102004043540A1 (de) * | 2004-09-09 | 2006-03-30 | Bayer Materialscience Ag | Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen |
-
2004
- 2004-09-09 DE DE200410043539 patent/DE102004043539A1/de not_active Withdrawn
-
2005
- 2005-08-27 ES ES05018640.2T patent/ES2614460T3/es not_active Expired - Lifetime
- 2005-08-27 EP EP05018640.2A patent/EP1634902B1/de not_active Expired - Lifetime
- 2005-09-01 US US11/217,727 patent/US9085656B2/en active Active
- 2005-09-02 CA CA 2518137 patent/CA2518137C/en not_active Expired - Fee Related
- 2005-09-08 TW TW94130806A patent/TWI391415B/zh not_active IP Right Cessation
- 2005-09-08 CN CN 200510099568 patent/CN1746244B/zh not_active Expired - Lifetime
- 2005-09-08 MX MXPA05009605 patent/MXPA05009605A/es active IP Right Grant
- 2005-09-09 JP JP2005262352A patent/JP4841906B2/ja not_active Expired - Fee Related
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